×
Aktivieren Sie Javascript in Ihrem Browser, um unsere Webseite optimal zu nutzen.
Dystrophin Antikörper
DMD
Reaktivität: Human, Maus, Ratte, Huhn
WB, IHC (p)
Wirt: Maus
Monoclonal
DYS-48
unconjugated
Produktnummer ABIN1107040
Produktdetails anti-Dystrophin Antikörper
(ausblenden)
Target
Alle Dystrophin (DMD) Antikörper anzeigen
Dystrophin (DMD)
Reaktivität
Alle Reaktivitäten für Dystrophin Antikörper
Human, Maus, Ratte, Huhn
Wirt
Alle Wirte für Dystrophin Antikörper
Maus
Klonalität
Alle Klonalitäten für Dystrophin Antikörper
Monoklonal
Konjugat
Alle Konjugate für Dystrophin Antikörper
Dieser Dystrophin Antikörper ist unkonjugiert
Applikation
Alle Applikationen für Dystrophin Antikörper
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
Spezifität
This antibody reacts to Dystrophin.
Aufreinigung
Affinity chromatography
Immunogen
Recombinant human dystrophin fragment.
Klon
DYS-48
Isotyp
IgG2b
Top Product
Discover our top product DMD Primärantikörper
Alternativen
(anzeigen)
Anwendungsinformationen
(ausblenden)
Applikationshinweise
Optimal working dilution should be determined by the investigator.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Handhabung
(ausblenden)
Rekonstitution
Restore with 1.2 % sodium acetate or neutral PBS
Konzentration
0,1 mg/mL
Buffer
1.2 % sodium acetate, with 2 mg BSA and 0.01 mg sodium azide as preservative.
Konservierungsmittel
Sodium azide
Vorsichtsmaßnahmen
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handhabung
Avoid repeated freezing and thawing.
Lagerung
-20 °C
Informationen zur Lagerung
Prior to reconstitution store at -20 °C. Following reconstitution store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
Details zu Dystrophin
(ausblenden)
Target
Dystrophin (DMD)
Andere Bezeichnung
Dystrophin / DMD (DMD Produkte )
Synonyme
DMD antikoerper, Dmd antikoerper, MGC83347 antikoerper, DKFZp459C1629 antikoerper, dmd antikoerper, MGC79631 antikoerper, DKFZp468A1620 antikoerper, Dp71 antikoerper, cb664 antikoerper, zfDYS antikoerper, im:6911785 antikoerper, zgc:110165 antikoerper, BMD antikoerper, CMD3B antikoerper, DXS142 antikoerper, DXS164 antikoerper, DXS206 antikoerper, DXS230 antikoerper, DXS239 antikoerper, DXS268 antikoerper, DXS269 antikoerper, DXS270 antikoerper, DXS272 antikoerper, DXSmh7 antikoerper, DXSmh9 antikoerper, Dp427 antikoerper, dys antikoerper, mdx antikoerper, pke antikoerper, DNADMD1 antikoerper, RATDMD antikoerper, CG17750 antikoerper, CG31175 antikoerper, CG34157 antikoerper, CG7240 antikoerper, CG7243 antikoerper, CG7344 antikoerper, DLP antikoerper, DLP1 antikoerper, DLP186 antikoerper, DLP2 antikoerper, DLP3 antikoerper, DmDLP antikoerper, DmDYS antikoerper, Dmel\\CG34157 antikoerper, Dp117 antikoerper, Dp186 antikoerper, Dp205 antikoerper, GI3046716 antikoerper, IDLP antikoerper, det antikoerper, dmDLP antikoerper, dmDp186 antikoerper, dmDys antikoerper, dystrophin antikoerper, dystrophin, gene 1 L homeolog antikoerper, dystrophin, gene 1 antikoerper, dystrophin, muscular dystrophy antikoerper, Dystrophin antikoerper, DMD antikoerper, LOC708073 antikoerper, dmd.1.L antikoerper, LOC465557 antikoerper, dmd.1 antikoerper, dmd antikoerper, Dmd antikoerper, Dys antikoerper
Hintergrund
Dystrophin(DMD) gene has 79 exons spanning at least 2,300 kb (2.3 Mb). The C terminus of the dystrophin protein is encoded by a highly conserved, alternatively spliced region of the gene. beta-dystroglycan binding activity is expressed by the dystrophin fragment spanning amino acids 3026-3345 containing the ZZ domain. DMD transcript is formed by at least 60 exons, the first half of the transcript is formed by a minimum of 33 exons spanning nearly 1000 kb, and the remaining portion has at least 27 exons that may spread over a similar distance. Dystrophin gene is expressed at a higher level in primary cultures of neuronal cells than in astro-glial cells derived from adult mouse brain.over expression of dystrophin prevents the development of the abnormal mechanical properties associated with dystrophic muscle without causing deleterious side effects.
Gen-ID
1756
NCBI Accession
NP_000100
UniProt
P11532
Pathways
Skeletal Muscle Fiber Development
Zuletzt angesehen
(ausblenden)